Developing mass spectrometry for the quantitative analysis of neuropeptides

被引:6
作者
Sauer, Christopher S. [1 ]
Phetsanthad, Ashley [1 ]
Riusech, Olga L. [1 ]
Li, Lingjun [1 ,2 ]
机构
[1] Univ Wisconsin Madison, Dept Chem, Madison, WI 53715 USA
[2] Univ Wisconsin Madison, Sch Pharm, Madison, WI 53715 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Imaging; Label-free; Mass Spectrometry; Multiplexing; Multi-omics; Neuropeptides; Peptidomics; PTMs; Quantitation; Stable Isotope Labeling; DATA-INDEPENDENT ACQUISITION; APPROACH ENABLED DISCOVERY; GLYCOSYLATED NEUROPEPTIDES; GLYCOPEPTIDE ANALYSIS; CRUSTACEAN HEMOLYMPH; PEPTIDES; QUANTIFICATION; IDENTIFICATION; PEPTIDOMICS; MS;
D O I
10.1080/14789450.2021.1967146
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Introduction Neuropeptides are signaling molecules originating in the neuroendocrine system that can act as neurotransmitters and hormones in many biochemical processes. Their exact function is difficult to characterize, however, due to dependence on concentration, post-translational modifications, and the presence of other comodulating neuropeptides. Mass spectrometry enables sensitive, accurate, and global peptidomic analyses that can profile neuropeptide expression changes to understand their roles in many biological problems, such as neurodegenerative disorders and metabolic function. Areas Covered We provide a brief overview of the fundamentals of neuropeptidomic research, limitations of existing methods, and recent progress in the field. This review is focused on developments in mass spectrometry and encompasses labeling strategies, post-translational modification analysis, mass spectrometry imaging, and integrated multi-omic workflows, with discussion emphasizing quantitative advancements. Expert Opinion Neuropeptidomics is critical for future clinical research with impacts in biomarker discovery, receptor identification, and drug design. While advancements are being made to improve sensitivity and accuracy, there is still room for improvement. Better quantitative strategies are required for clinical analyses, and these methods also need to be amenable to mass spectrometry imaging, post-translational modification analysis, and multi-omics to facilitate understanding and future treatment of many diseases.
引用
收藏
页码:607 / 621
页数:15
相关论文
共 160 条
[1]   PACAP and Other Neuropeptide Targets Link Chronic Migraine and Opioid-induced Hyperalgesia in Mouse Models [J].
Anapindi, Krishna D. B. ;
Yang, Ning ;
Romanova, Elena V. ;
Rubakhin, Stanislav S. ;
Tipton, Alycia ;
Dripps, Isaac ;
Sheets, Zoie ;
Sweedler, Jonathan V. ;
Pradhan, Amynah A. .
MOLECULAR & CELLULAR PROTEOMICS, 2019, 18 (12) :2447-2458
[2]   Improving Proteome Coverage on a LTQ-Orbitrap Using Design of Experiments [J].
Andrews, Genna L. ;
Dean, Ralph A. ;
Hawkridge, Adam M. ;
Muddiman, David C. .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2011, 22 (04) :773-783
[3]   Perspectives on ethnic and racial disparities in Alzheimer's disease and related dementias: Update and areas of immediate need [J].
Babulal, Ganesh M. ;
Quiroz, Yakeel T. ;
Albensi, Benedict C. ;
Arenaza-Urquijo, Eider ;
Astell, Arlene J. ;
Babiloni, Claudio ;
Bahar-Fuchs, Alex ;
Bell, Joanne ;
Bowman, Gene L. ;
Brickman, Adam M. ;
Chetelat, Gael ;
Ciro, Carrie ;
Cohen, Ann D. ;
Dilworth-Anderson, Peggye ;
Dodge, Hiroko H. ;
Dreux, Simone ;
Edland, Steven ;
Esbensen, Anna ;
Evered, Lisbeth ;
Ewers, Michael ;
Fargo, Keith N. ;
Fortea, Juan ;
Gonzalez, Hector ;
Gustafson, Deborah R. ;
Head, Elizabeth ;
Hendrix, James A. ;
Hofer, Scott M. ;
Johnson, Leigh A. ;
Jutten, Roos ;
Kilborn, Kerry ;
Lanctot, Krista L. ;
Manly, Jennifer J. ;
Martins, Ralph N. ;
Mielke, Michelle M. ;
Morris, Martha Clare ;
Murray, Melissa E. ;
Oh, Esther S. ;
Parra, Mario A. ;
Rissman, Robert A. ;
Roe, Catherine M. ;
Santos, Octavio A. ;
Scarmeas, Nikolaos ;
Schneider, Lon S. ;
Schupf, Nicole ;
Sikkes, Sietske ;
Snyder, Heather M. ;
Sohrabi, Hamid R. ;
Stern, Yaakov ;
Strydom, Andre ;
Tang, Yi .
ALZHEIMERS & DEMENTIA, 2019, 15 (02) :292-312
[4]  
Beaudry F, 2018, BIOMED CHROMATOGR, V32, P1
[5]   Deciphering the Role of EGL-3 for Neuropeptides Processing in Caenorhabditis elegans Using High-Resolution Quadrupole-Orbitrap Mass Spectrometry [J].
Ben Salem, Jennifer ;
Nkambeu, Bruno ;
Arvanitis, Dina N. ;
Beaudry, Francis .
NEUROCHEMICAL RESEARCH, 2018, 43 (11) :2121-2131
[6]   Amodal Aspects of Linguistic Design [J].
Berent, Iris ;
Dupuis, Amanda ;
Brentari, Diane .
PLOS ONE, 2013, 8 (04)
[7]   ProSAAS-derived peptides are regulated by cocaine and are required for sensitization to the locomotor effects of cocaine [J].
Berezniuk, Iryna ;
Rodriguiz, Ramona M. ;
Zee, Michael L. ;
Marcus, David J. ;
Pintar, John ;
Morgan, Daniel J. ;
Wetsel, William C. ;
Fricker, Lloyd D. .
JOURNAL OF NEUROCHEMISTRY, 2017, 143 (03) :268-281
[8]   Structural characterization of arginine vasopressin and lysine vasopressin by Fourier-transform ion cyclotron resonance mass spectrometry and infrared multiphoton dissociation [J].
Bianco, Giuliana ;
Battista, Fabio G. ;
Buchicchio, Alessandro ;
Amarena, Concetta G. ;
Schmitt-Kopplin, Philippe ;
Guerrieri, Antonio .
EUROPEAN JOURNAL OF MASS SPECTROMETRY, 2015, 21 (03) :211-219
[9]   Processing strategies and software solutions for data-independent acquisition in mass spectrometry [J].
Bilbao, Aivett ;
Varesio, Emmanuel ;
Luban, Jeremy ;
Strambio-De-Castillia, Caterina ;
Hopfgartner, Gerard ;
Mueller, Markus ;
Lisacek, Frederique .
PROTEOMICS, 2015, 15 (5-6) :964-980
[10]  
Boonen K, 2018, METHODS MOL BIOL, V1719, P141, DOI 10.1007/978-1-4939-7537-2_9